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Year Number of Results
1998 1
1999 1
2000 1
2001 1
2006 1
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2010 1
2013 1
2014 2
2017 2
2022 1
2024 0

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Page 1
Investigation of the felodipine glassy state by atomic force microscopy.
Trojak A, Kocevar K, Musevic I, Srcic S. Trojak A, et al. Int J Pharm. 2001 May 7;218(1-2):145-51. doi: 10.1016/s0378-5173(01)00625-1. Int J Pharm. 2001. PMID: 11337158
The glassy state of felodipine was prepared by melting crystals of felodipine on a clean glass slide and cooling to room temperature. ...Crystallization occurred slowly and spontaneously at room temperature, below the glassy state transition temperature (Tg). The co …
The glassy state of felodipine was prepared by melting crystals of felodipine on a clean glass slide and cooling to room temperature. …
Predicting Drug Release Rate of Implantable Matrices and Better Understanding of the Underlying Mechanisms through Experimental Design and Artificial Neural Network-Based Modelling.
Benkő E, Ilič IG, Kristó K, Regdon G Jr, Csóka I, Pintye-Hódi K, Srčič S, Sovány T. Benkő E, et al. Pharmaceutics. 2022 Jan 19;14(2):228. doi: 10.3390/pharmaceutics14020228. Pharmaceutics. 2022. PMID: 35213961 Free PMC article.
The data obtained were used to construct models based on artificial neural networks (ANNs) to predict drug dissolution. FT-IR studies confirmed the presence of H-bond-based solid-state interactions that intensified during dissolution. These results confirmed our hypothesis …
The data obtained were used to construct models based on artificial neural networks (ANNs) to predict drug dissolution. FT-IR studies confir …
Application of 14N NQR to the study of piroxicam polymorphism.
Lavrič Z, Pirnat J, Lužnik J, Seliger J, Zagar V, Trontelj Z, Srčič S. Lavrič Z, et al. J Pharm Sci. 2010 Dec;99(12):4857-65. doi: 10.1002/jps.22186. J Pharm Sci. 2010. PMID: 20597116
The (14)N NQR method has the potential to become an additional and important spectroscopic tool in the study of solid-state forms, not only of pure active pharmaceutical ingredients or excipients, but also of their mixtures. ...
The (14)N NQR method has the potential to become an additional and important spectroscopic tool in the study of solid-state forms, no …
Physico-chemical characterisation of different clindamycin phosphate samples.
Vranić E, Planinsek O, Tivadar A, Hadzović S, Srcic S. Vranić E, et al. Bosn J Basic Med Sci. 2007 May;7(2):180-7. doi: 10.17305/bjbms.2007.3078. Bosn J Basic Med Sci. 2007. PMID: 17489758 Free article.
For the majority of the pharmaceutical dosage forms, the substances that are used maintain solid state under the standard storage conditions, i.e. powders. The interactions of pharmaceutical powders (active ingredient(s) and excipients) with liquids and vapors (particularl …
For the majority of the pharmaceutical dosage forms, the substances that are used maintain solid state under the standard storage con …
EMA and EFSA Joint Scientific Opinion on measures to reduce the need to use antimicrobial agents in animal husbandry in the European Union, and the resulting impacts on food safety (RONAFA).
EMA Committee for Medicinal Products for Veterinary Use (CVMP) and EFSA Panel on Biological Hazards (BIOHAZ); Murphy D, Ricci A, Auce Z, Beechinor JG, Bergendahl H, Breathnach R, Bureš J, Duarte Da Silva JP, Hederová J, Hekman P, Ibrahim C, Kozhuharov E, Kulcsár G, Lander Persson E, Lenhardsson JM, Mačiulskis P, Malemis I, Markus-Cizelj L, Michaelidou-Patsia A, Nevalainen M, Pasquali P, Rouby JC, Schefferlie J, Schlumbohm W, Schmit M, Spiteri S, Srčič S, Taban L, Tiirats T, Urbain B, Vestergaard EM, Wachnik-Święcicka A, Weeks J, Zemann B, Allende A, Bolton D, Chemaly M, Fernandez Escamez PS, Girones R, Herman L, Koutsoumanis K, Lindqvist R, Nørrung B, Robertson L, Ru G, Sanaa M, Simmons M, Skandamis P, Snary E, Speybroeck N, Ter Kuile B, Wahlström H, Baptiste K, Catry B, Cocconcelli PS, Davies R, Ducrot C, Friis C, Jungersen G, More S, Muñoz Madero C, Sanders P, Bos M, Kunsagi Z, Torren Edo J, Brozzi R, Candiani D, Guerra B, Liebana E, Stella P, Threlfall J, Jukes H. EMA Committee for Medicinal Products for Veterinary Use (CVMP) and EFSA Panel on Biological Hazards (BIOHAZ), et al. EFSA J. 2017 Jan 24;15(1):e04666. doi: 10.2903/j.efsa.2017.4666. eCollection 2017 Jan. EFSA J. 2017. PMID: 32625259 Free PMC article.
Reduction strategies have been implemented successfully in some Member States. Such strategies include national reduction targets, benchmarking of antimicrobial use, controls on prescribing and restrictions on use of specific critically important antimicrobials, together w …
Reduction strategies have been implemented successfully in some Member States. Such strategies include national reduction targets, be …
Melt granulation in fluidized bed: a comparative study of spray-on versus in situ procedure.
Mašić I, Ilić I, Dreu R, Ibrić S, Parojčić J, Srčič S. Mašić I, et al. Drug Dev Ind Pharm. 2014 Jan;40(1):23-32. doi: 10.3109/03639045.2012.744415. Epub 2013 Jan 7. Drug Dev Ind Pharm. 2014. PMID: 23294368
In the in situ experiments, the influence of binder particle size and binder content was evaluated. Solid-state characterization was performed by means of differential scanning calorimetry, X-ray powder diffraction and Fourier transform infrared spectroscopy. ...Paracetamo …
In the in situ experiments, the influence of binder particle size and binder content was evaluated. Solid-state characterization was …
Some physicochemical properties of 7-oxoacyl-L-alanyl-D-isoglutamines.
Planinsek O, Srcic S. Planinsek O, et al. Int J Pharm. 1999 Oct 5;187(2):199-207. doi: 10.1016/s0378-5173(99)00192-1. Int J Pharm. 1999. PMID: 10502626
From the true density and melting enthalpy measurements it is evident that with the increase of alkyl chain the arrangement of molecules in solid state is increasing up to the molecule with four methylene groups between terminal methyl and 7-oxo group. ...
From the true density and melting enthalpy measurements it is evident that with the increase of alkyl chain the arrangement of molecules in …
Novel hybrid silica xerogels for stabilization and controlled release of drug.
Maver U, Godec A, Bele M, Planinsek O, Gaberscek M, Srcic S, Jamnik J. Maver U, et al. Int J Pharm. 2007 Feb 7;330(1-2):164-74. doi: 10.1016/j.ijpharm.2006.09.024. Epub 2006 Sep 23. Int J Pharm. 2007. PMID: 17055199
PURPOSE: The goal was to show that incorporation of a model drug into a porous solid matrix with small enough pores should lead to composites in which the drug would be in the amorphous rather than in the crystalline state. Due to spatial constraints, the amorphous stat
PURPOSE: The goal was to show that incorporation of a model drug into a porous solid matrix with small enough pores should lead to composite …
13 results